Primary Site >> Stomach Cancer

Gene >> PLEKHO1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000369124
Start 150159161:150159161(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.868C>T
AA Mutation p.Arg290Trp(p.R290W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000369124
Start 150156178:150156178(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.290T>G
AA Mutation p.Leu97Arg(p.L97R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000369124
Start 150156082:150156082(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.194A>C
AA Mutation p.Asn65Thr(p.N65T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000369124
Start 150156120:150156120(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.232T>C
AA Mutation p.Cys78Arg(p.C78R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000369124
Start 150159493:150159493(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs587658515
CDS Mutation c.1200G>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000369124
Start 150159394:150159394(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1101C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000369124
Start 150159054:150159054(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.766delC
AA Mutation p.Gln256ArgfsTer6(p.Q256Rfs*6)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000369124
Start 150156106:150156107(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.219_264dupTGACTATGAGAAGTGTGAAGAGCTCCGGAAGTCCAAGAGCAGGAGC
AA Mutation p.Lys89Ter(p.K89*)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000369124
Start 150159026:150159027(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.739dupA
AA Mutation p.Thr247AsnfsTer46(p.T247Nfs*46)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript